Mathematical Intelligence Application Lab, Institute for Mathematical Sciences, School of Math, Renmin University of China, Beijing, 100872, China.
Interdiscip Sci. 2020 Jun;12(2):204-216. doi: 10.1007/s12539-020-00364-w. Epub 2020 Mar 17.
Protein-protein interactions are important for most biological processes and have been studied for decades. However, the detailed formation mechanism of protein-protein interaction interface is still ambiguous, which makes it difficult to accurately predict the protein-protein interaction interface residue pairs. Here, we extract the interface residue-residue contacts from the decoys in the ZDOCK protein-protein complex decoy set with RMSD mostly larger than 3 Å. To accurately compute the interface residue-residue contacts, we define a new constant called interface residue pairs frequency, which counts the atom contact numbers between two interface residues. We normalize interface residue pairs frequency to pick out the top residue-residue pairs from all the possible pairs preferential to be on correct protein-protein interaction interface. When tested on 37 protein dimers from the decoy set where most decoys are incorrect, our method successfully predicts 30 protein dimers with a success rate of up to 81.1%. Higher accuracy than some other state-of-the-art methods confirmed the performance of our method.
蛋白质-蛋白质相互作用对大多数生物过程都很重要,并且已经研究了几十年。然而,蛋白质-蛋白质相互作用界面的详细形成机制仍然不清楚,这使得准确预测蛋白质-蛋白质相互作用界面残基对变得困难。在这里,我们从 ZDOCK 蛋白质-蛋白质复合物诱饵集中 RMSD 大多大于 3Å 的诱饵中提取界面残基-残基接触。为了准确计算界面残基-残基接触,我们定义了一个新的常数,称为界面残基对频率,它计算两个界面残基之间的原子接触数。我们对界面残基对频率进行归一化,从所有可能的残基对中挑选出优先出现在正确蛋白质-蛋白质相互作用界面上的残基对。在对诱饵集中的 37 个蛋白质二聚体进行测试时,其中大多数诱饵都是不正确的,我们的方法成功地预测了 30 个蛋白质二聚体,成功率高达 81.1%。比其他一些最先进的方法更高的准确性证实了我们方法的性能。